STX16-MYT1 Fusion FISH Probe
The STX16-MYT1 Fusion FISH Probe is used to confirm a fusion of the STX16 and MYT1 genes. The fusion of the STX16 and MYT1 genes has been associated with Breast Invasive Carcinoma. These probes are FISH confirmed on normal peripheral blood in both interphase nuclei and metaphase spreads before shipment. Typical turnaround time for this product is 7-14 days after purchase.
** This product is for in vitro and research use only. This product is not intended for diagnostic use. Please note that both genes fall on the same chromosome and inter-chromosomal detection may be difficult to detect depending on the genes proximity to one another. Please consult our support staff before ordering this product to ensure that the probe can be designed to meet your specific needs.
| SKU | Test Kits | Buffer | Dye Color | Order Now |
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| STX16-MYT1-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| STX16-MYT1-20-RERE | 20 (40 μL) | 200 μL |
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| STX16-MYT1-20-REOR | 20 (40 μL) | 200 μL |
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| STX16-MYT1-20-REGO | 20 (40 μL) | 200 μL |
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| STX16-MYT1-20-REGR | 20 (40 μL) | 200 μL |
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| STX16-MYT1-20-REAQ | 20 (40 μL) | 200 μL |
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| STX16-MYT1-20-ORRE | 20 (40 μL) | 200 μL |
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| STX16-MYT1-20-OROR | 20 (40 μL) | 200 μL |
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| STX16-MYT1-20-ORGO | 20 (40 μL) | 200 μL |
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| STX16-MYT1-20-ORAQ | 20 (40 μL) | 200 μL |
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| STX16-MYT1-20-GORE | 20 (40 μL) | 200 μL |
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| STX16-MYT1-20-GOOR | 20 (40 μL) | 200 μL |
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| STX16-MYT1-20-GOGO | 20 (40 μL) | 200 μL |
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| STX16-MYT1-20-GOGR | 20 (40 μL) | 200 μL |
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| STX16-MYT1-20-GOAQ | 20 (40 μL) | 200 μL |
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| STX16-MYT1-20-GRRE | 20 (40 μL) | 200 μL |
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| STX16-MYT1-20-GROR | 20 (40 μL) | 200 μL |
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| STX16-MYT1-20-GRGO | 20 (40 μL) | 200 μL |
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| STX16-MYT1-20-GRGR | 20 (40 μL) | 200 μL |
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| STX16-MYT1-20-GRAQ | 20 (40 μL) | 200 μL |
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| STX16-MYT1-20-AQRE | 20 (40 μL) | 200 μL |
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| STX16-MYT1-20-AQOR | 20 (40 μL) | 200 μL |
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| STX16-MYT1-20-AQGO | 20 (40 μL) | 200 μL |
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| STX16-MYT1-20-AQGR | 20 (40 μL) | 200 μL |
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| STX16-MYT1-20-AQAQ | 20 (40 μL) | 200 μL |
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MYT1 Gene Summary
The protein encoded by this gene is a member of a family of neural specific, zinc finger-containing DNA-binding proteins. The protein binds to the promoter regions of proteolipid proteins of the central nervous system and plays a role in the developing nervous system. [provided by RefSeq, Jul 2008]
Gene Name: Myelin Transcription Factor 1
Chromosome: CHR20: 62795826 -62873606
Locus: 20q13.33
STX16 Gene Summary
This gene encodes a protein that is a member of the syntaxin or t-SNARE (target-SNAP receptor) family. These proteins are found on cell membranes and serve as the targets for V-SNARES (vesicle-SNAP receptors) permitting specific synaptic vesicle docking and fusion. A microdeletion in the region of chromosome 20 where this gene is located has been associated with pseudohypoparathyroidism type Ib. Multiple transcript variants have been found for this gene. Read-through transcription also exists between this gene and the neighboring downstream aminopeptidase-like 1 (NPEPL1) gene. [provided by RefSeq, Mar 2011]
Gene Name: Syntaxin 16
Chromosome: CHR20: 57226308 -57254582
Locus: 20q13.32
Gene Diseases
The STX16 MYT1 Fusion has been associated with the following diseases:
| Disease Name |
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| Breast Invasive Carcinoma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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